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benztropine mesylate
benztropine mesylate - 67046-042-30 - (benztropine mesylate)
Drug Information of benztropine mesylate
| Product NDC: | 67046-042 |
| Proprietary Name: | benztropine mesylate |
| Non Proprietary Name: | benztropine mesylate |
| Active Ingredient(s): | 1 mg/1 & nbsp; benztropine mesylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of benztropine mesylate
| Product NDC: | 67046-042 |
| Labeler Name: | Contract Pharmacy Services-PA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040103 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100628 |
Package Information of benztropine mesylate
| Package NDC: | 67046-042-30 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (67046-042-30) |
NDC Information of benztropine mesylate
| NDC Code | 67046-042-30 |
| Proprietary Name | benztropine mesylate |
| Package Description | 30 TABLET in 1 BLISTER PACK (67046-042-30) |
| Product NDC | 67046-042 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benztropine mesylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100628 |
| Marketing Category Name | ANDA |
| Labeler Name | Contract Pharmacy Services-PA |
| Substance Name | BENZTROPINE MESYLATE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA] |
